| Literature DB >> 29277325 |
Yanhui Jia1, Zhenzhen Li1, Weixia Cai1, Dan Xiao1, Shichao Han1, Fu Han1, Xiaozhi Bai1, Kejia Wang1, Yang Liu1, Xiaoqiang Li1, Hao Guan2, Dahai Hu3.
Abstract
Molecular mechanisms for macrophage immune responses modulated by SIRT1 during sepsis remain unclear. Here, we show that SIRT1 expression is down-regulated in macrophages from mouse sepsis model or LPS stimulation. SIRT1 expression in macrophages correlates with low levels of a long noncoding RNA (lncRNA)-NONMMUT003701 [named as lncRNA-CCL2]. SIRT1 inhibits lncRNA-CCL2 expression via sustaining a repressive chromatin state in the lncRNA-CCL2 locus. The inflammation cytokines expression is downregulated by knockdown of lncRNA-CCL2. Such inhibition can be reversed partly by decreased SIRT1 activity. Thus, this work uncovers previously unidentified mechanisms in which SIRT1 associates with lncRNA and lncRNA regulates macrophage inflammatory response.Entities:
Keywords: Inflammation cytokines; Macrophages; SIRT1; Sepsis; lncRNA
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Year: 2017 PMID: 29277325 DOI: 10.1016/j.bbadis.2017.12.029
Source DB: PubMed Journal: Biochim Biophys Acta Mol Basis Dis ISSN: 0925-4439 Impact factor: 5.187